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1.
  • 1.1. Healthy 6- to 12-day-old Heliothis zea (bollworm) larvae showed a mean oxygen uptake of 3.1 μl O2/mg body wt per hr.
  • 2.2. Similar larvae infected with the fungus Nomuraea rileyi had a mean uptake of 4.01 μl O2/mg per hr.
  • 3.3. The weights of the two groups of insects did not differ.
  • 4.4. T-test showed a significant (P < 0.01) difference in oxygen uptake between healthy and infected larvae.
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2.
  • 1.1. Simultaneous measurement of calcium fluxes in brown trout, at low external [Ca] (20 μ mol 1−1), provided evidence of active uptake of Ca from the medium.
  • 2.2. At pH 4.5, calcium influx was inhibited and efflux was stimulated.
  • 3.3. Cd and Mn, but not Al, at concentrations within the ranges found in acid waters experiencing fish population decline, inhibited calcium influx. Efflux was unaffected.
  • 4.4. Cd and Mn stimulated sodium influx and efflux.
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3.
  • 1.1. The objective of the present study was to determine the effect of age and taurine on chick B cell calcium uptake and membrane (Ca2+ + Mg2+)-ATPase activity in 1–4-week-old chicks.
  • 2.2. The calcium uptake rate decreased with age (P < 0.05) and was further decreased by taurine (P < 0.05).
  • 3.3. (Ca2+ + Mg2+)-ATPase activity increased with age (P < 0.05) and was stimulated by taurine (P < 0.05).
  • 4.4. The data demonstrate that the flux of calcium across the B-cell membrane changes during early post-hatch development, and that taurine regulates both the influx and efflux of calcium in chick B-cells.
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4.
  • 1.1. Longitudinally split or completely regenerated branch tips from Leplogorgia virgulata show no differences in calcium uptake between control and ouabain treatments. This indicates that there is no ouabain sensitive Na+, K+-ATPase involved in calcium uptake.
  • 2.2. The tissue fractions of both regenerated and split branch tips show, at certain times, higher calcium uptake than control fractions. In the spicule fractions of these tips calcium uptake decreases in vandate treated specimens.
  • 3.3. Pulse-chase experiments show an initial rapid release of calcium from the tips into surrounding seawater.
  • 4.4. The results may suggest the presence of outwardly directed calcium pumps on the basal/lateral and apical plasma membranes of the epithelial cells. Outwardly directed calcium pumps may also be envisaged on the cell membranes of scleroblasts. In addition, pumps may move calcium into specific organelles of the scleroblasts en route to the spicule forming vacuoles.
  • 5.5. These pumps are likely to be Ca2+-ATPase.
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5.
  • 1.1. The amount of sugar required for growth of Heliothis zea larvae on a chemically defined diet was determined.
  • 2.2. Larvae grew well on fructose, galactose, sucrose, trehalose and raffinose diets but not on diets containing more than 0.5% glucose.
  • 3.3. A starch diet did not promote rapid larval growth.
  • 4.4. Hemolymph trehalose levels in 12-day-old larvae ranged from none to 45μmoles/ml.
  • 5.5. A method for analysis of hemolymph trehalose by gas chromatography is described.
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6.
  • 1.1. The midge larva (Chironomus yoshimatsui) exposed to cadmium (10 μg Cd/ml) for 2 days was histochemically stained with benzothiazolylazo-β-naphthol.
  • 2.2. A large portion of cadmium taken up by the larvae was distributed to the digestive tract, epithelial tract and fat bodies.
  • 3.3. Cadmium accumulated in the fat bodies was discharged slowly relative to cadmium in the tract contents when the larvae were placed in control water.
  • 4.4. Glycogen in the fat bodies of cadmium-exposed larvae was insensitive to PAS staining.
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7.
  • 1.1. Responses of channel catfish (Ictalurus punctatus) swim-up fry to dietary calcium in soft (< 1 mg/1 as CaCO3) and hard (> 100 mg/1 as CaCO3) water were determined by feeding purified egg-white diets containing 0, 0.5, 1.0, or 2.0% calcium from CaCO3 for 8 weeks.
  • 2.2. Catfish fry fed the basal diet (0.03% Ca) in hard and soft water had lower whole-body ash and whole-body calcium concentrations but higher weight gain and survival than those fed calcium-supplemented diets.
  • 3.3. Fry in soft water generally had lower whole-body ash, whole-body calcium, and survival, as well as a higher incidence of spinal deformities than fry in hard water.
  • 4.4. Feeding higher levels of calcium to fry reared in soft water did not increase whole-body calcium levels or decrease spinal deformities to the levels observed for fry reared in hard water and fed supplemental calcium.
  • 5.5. These data indicate that calcium derived solely from dietary or environmental sources was not sufficient for optimum health of channel catfish fry.
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8.
  • 1.1. Polyamines were extracted from the guts and ovaries of the sea urchin Anthocidoris crassispina, and the guts and flesh of the sea cucumber Stichopus japonicus and the sea squirt Halocynthia roretzi, the oyster Crassostrea gigas and the short-necked clam Tapes philippinarum, and analyzed by ion-exchange high-performance liquid chromatography and gas chromatography-mass spectrometry.
  • 2.2. Norspermidine and norspermine as well as putrescine, cadaverine, spermidine, spermine and agmatine were the ubiquitous polyamines in these invertebrates. These results suggest the widespread distribution of norspermidine and norspermine in invertebrates.
  • 3.3. Thermopentamine, thermohexamine and homothermohexamine were found in the sea urchin. This in the first report on the occurence of thermopentamine and hexaamine in invertebrates.
  • 4.4. Homospermidine, canavalmine, aminopropylhomospermidine, homospermine, caldopentamine, homocaldopentamine and aminopropylcanavalmine were found in the sea cucumber. Homospermidine, aminopropylhomospermidine and homospermine were found in the squirt. This is the first report on the occurence of canavalmine, aminopropylhomospermidine, homospermine, homocaldopentamine and aminopropylcanavalmine in invertebrates.
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9.
  • 1.1. Cutaneous O2 uptake in the carp, Cyprinus carpio, was determined at various water flow rates across the skin (.V) ranging from 2.5 to 40 ml/min, using flow-through respirometers.
  • 2.2. When thickness of water flow was 2mm, cutaneous O2 uptake remained stable (about 3.8 nmol/cm2/min) at a .V of 20–40 ml/min and decreased with .V below 20 ml/min.
  • 3.3. When thickness of water flow was 4 mm, cutaneous O2 uptake decreased with .V below 40 ml/min.
  • 4.4. Apparent water velocity (U') was calculated dividing .V by an area of a cross section of the water flow (0.5 and 1.0 cm2 respectively). In both experiments, cutaneous O2 uptake decreased with U' below 0.7 cm/sec.
  • 5.5. This suggests that cutaneous O2 uptake in the carp is limited at a low water velocity by a resistance of the hypoxic boundary layer.
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10.
  • 1.1. Mitochondria with high respiratory control ratios (RCR) have been isolated from the ventricle of the marine clam Mercenaria mercenaria.
  • 2.2. Proline is the preferred substrate of the mitochondria of the ventricle based on state 3 rates.
  • 3.3. Pyruvate, ornithine and succinate are oxidized at rates 3/4 that of proline.
  • 4.4. α-Glycerophosphate was oxidized at rates 1/2 that of proline.
  • 5.5. The pH optimum for proline oxidation lies between 6.5 and 7.5 based on RCR and ADP/O and between 7.0 and 7.4 based on state 3 rates.
  • 6.6. KCl concentrations between 250 and 450 mM gave optimal values for the oxidation of proline based on RCR and state 3 rates.
  • 7.7. KCl concentration had little effect on ADP/O between 100 and 850 mM.
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11.
  • 1.1. Cadmium (Cd) and zinc (Zn) were inhibitory to calcium uptake by isolated gills of Fundulus heteroclitus in vitro. The metals appeared to act by displacing Ca2+ ions from protein carriers involved in facilitated diffusion.
  • 2.2. In saltwater fish, transport of calcium across the serosal membrane of gill chloride cells is partly energy dependent and is likely mediated by Ca2+-ATPase. However, much of the calcium transport through the gill epithelium appears to occur by passive processes.
  • 3.3. Cd (10−5M—10−3M) and Zn (10−7M—10−3 M) inhibited calcium uptake by isolated scale patches incubated in a physiological saline.
  • 4.4. Cyanide, oubain, and quercetin treatment of scale patches produced results similar to those of the Cd and Zn treatments suggesting that metal-induced inhibition of ATPases may be responsible for reduced calcium transport by scale osteoblasts.
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12.
  • 1.1. The role of aldosterone on active potassium transport across lizard colon under voltage-clamped conditions has been investigated.
  • 2.2. Control colons exhibited no net potassium flux (Jknet) despite of the existence of active opposite unidi ectional fluxes.
  • 3.3. An important net secretory potassium flux was found in short-circuited aldosterone-stimulated colons.
  • 4.4. Mucosal amiloride did not change (Jknet) either in control or aldosterone-stimulated colons.
  • 5.5. Luminal barium alters K + transport in a manner consistent with the presence of barium-sensitive conductances at the apical membrane of both control and aldosterone-treated colons.
  • 6.6. The effects of ouabain and barium on control and aldosterone-induced potassium flows were consistent with a model involving basolateral uptake by an Na +-K +-ATPase and conductive exit across the apical membrane.
  • 7.7. The stimulatory effect of aldosterone on potassium secretion is associated with parallel increases of both basolateral K + entry and the apical conductive pathway.
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13.
  • 1.1. The content of atrial natriuretic peptides (ANPs) in the auricles of oysters, Crassostrea virginica, was significantly (P < 0.01) greater than in their ventricles.
  • 2.2. High-performance gel permeation chromatography (HP-GPC) followed by ANF radioimmunoassay revealed two peaks in both oyster and vertebrate (rat) hearts—a major peak where the 12.6–14 kDa ANF prohormone elutes and a smaller peak where the pure human form of ANF elutes.
  • 3.3. HP-GPC evaluation followed by proANF 31–67 radioimmunoassay revealed only an ANF-like prohormone while HP-GPC followed by proANF 1–30 radioimmunoassay revealed the ANF prohormone and a proANF 1–30-like peptide in oyster and rat hearts.
  • 4.4. ANPs concentrations in hemolymph were 940 ± 129, 225 ± 25, and 100 ± 10 pg/ml by the proANF 1–30, proANF 31–67, and ANF radioimmunoassays, respectively.
  • 5.5. Atrial natriuretic-like peptides are present in the oyster heart in molecular species similar to vertebrate species and these peptides are also present in hemolymph.
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14.
  • 1.1. 14C-dichlorofarnesoate permeated rapidly into Haemonchus contortus (infective juveniles) and Panagrellus redivivus (mixed cultures) and was strongly bound by hydrophobic association (Ks > 10−4M).
  • 2.2. Uptake rose linearly with increases in temperature (5–38°C) and external concentration (C0; 0.07–2.15 × 10−4 M). Within 1 hr the internal concentration, C1 was >C C0.
  • 3.3. The pH of the medium (6–8) did not affect uptake.
  • 4.4. Efflux of dichlorofarnesoate was low: the half-time of release was > 18 hr.
  • 5.5. The uptake curve approximated to the expression C1/C0 = a(1 − e−bt) with a and b as constants and t in hr.
  • 6.6. These results clarify previous work on the inhibitory action of juvenile hormone on the development of nematodes.
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15.
  • 1.1. A starvation test was conducted in small beakers with stage 1 (S1) and stage 2 (S2) Macrobrachium rosenbergii larvae to determine optimal salinities.
  • 2.2. Experiments were first performed with S2 larvae at 13 ppt to identify a suitable medium made with artificial sea salts.
  • 3.3. A broad-range (0–35 ppt) and a subsequent narrow-range (9–16 ppt) salinity experiment with S2 larvae were used to identify 13 ppt as the optimal salinity, with 12 ppt as the next best; this agrees well with most previous estimates of optimal salinities for rearing larvae.
  • 4.4. S1 larvae were also tested in a narrow-range salinity experiment but were not used further because, unlike starved S2 larvae, they molted during the experiment.
  • 5.5. Identification of the optimal salinity was not affected by 50% daily water exchange or by bright light.
  • 6.6. Exposure of larvae to three different salinities—7, 13 and 19 ppt—during S1 influenced the width of the optimal salinity range for S2 larvae.
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16.
  • 1.1. Vesicles from the sarcoplasmic reticulum of lobster muscle accumulate Ca2+ if supplied with ATP as an energy source. A search was undertaken for inhibitors of Ca2+ transport.
  • 2.2. p-Hydroxymercuribenzoate can completely inhibit Ca2+ transport and ATP hydrolysis. 2–4 Dinitrophenol inhibits uptake but not hydrolysis.
  • 3.3. Sr2+, Ba2+ and Zn2+ inhibit uptake, perhaps by competing with Ca2+ for a carrier.
  • 4.4. The vesicles contain acetylcholinesterase. Anticholinesterases can reduce —but not abolish—Ca2+ uptake. Acetylcholine has no effect on the activity of the vesicles.
  • 5.5. Ca2+ uptake is not affected by Mn2+, glutamate, pilocarpine, carnosine, caffeine, strophanthidin or tetraethylammonium.
  • 6.6. K+ is needed for maximal activity of the uptake system but not for ATP hydrolysis. Apparently K+ enhances the coupling between the energy supply and the carrier mechanism.
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17.
  • 1.1. Nereis pharangeal visceral muscle is composed of obliquely striated fibres with low mitochondrial density and moderately developed sarcoplasmic reticulum.
  • 2.2. Isolated mitochondria and sarcoplasmic reticulum showed moderate passive calcium binding but only low ATP-promoted calcium binding which was inhibited by caffeine.
  • 3.3. Whole fibres preloaded with Ca45 showed a two compartment efflux. The slow, presumably intracellular, compartment accounted for only 10% of total Ca45 activity.
  • 4.4. Both acetylcholine and high KCl treatments stimulated calcium influx, causing contractures while calcium-free and EGTA treatments inhibited both these contractures and normal spontaneous contractions.
  • 5.5. Lanthanum inhibited normal contractility and KCl contractures. Lanthanum also inhibited Ca45 influx but was without effect on Ca45 efflux.
  • 6.6. It is concluded that there is little calcium storage capacity in these visceral muscle fibres and that normal contractions are strongly dependent upon extracellular calcium influx.
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18.
  • 1.1. Isolated mitochondria from rat liver were incubated in the presence of [U-14C]palmitate, ATP, CoA, carnitine, EGTA (ethylene glycol bis (β-aminoethyl ether) N,N′-tetraacetic acid) and varying amounts of calcium.
  • 2.2. When a KCl-based incubation medium was used, the oxidation of palmitate was inhibited when the concentration of free calcium was increased from about 0.1–10μM.
  • 3.3. When a sucrose-based incubation medium was used, the basal rate of palmitate oxidation was about half of that observed with the KCl-medium and calcium had a stimulatory effect.
  • 4.4. With the KCl-medium the rate of oxygen consumption was inhibited by calcium with α-ketoglutarate as well as palmitate as the respiratory substrate.
  • 5.5. No inhibitory effect of calcium was observed with succinate or β-hydroxybutyrate.
  • 6.6. With the KCl-medium and with α-ketoglutarate as the respiratory substrate, state 3 respiration but not state 4 respiration was inhibited by calcium.
  • 7.7. When the sucrose-medium was used, state 3 respiration was first inhibited by calcium, but this inhibition was gradually relieved and the respiratory rate finally became higher than it was before calcium addition.
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19.
  • 1.1. Eyestalk unablated and unilaterally ablated Penaeus monodon juveniles had survival rates after 5 months of 75–72.5 and 67.5–60%, respectively.
  • 2.2. Unilaterally ablated shrimps had significantly higher (P < 0.05) growth rate than unablated shrimps.
  • 3.3. Eyestalk-ablatement resulted in a decrease in the haemolymph sodium concentration and an increase in the potassium and calcium concentration of shrimps.
  • 4.4. The osmolarity of haemolymph and total protein concentration of unablated shrimps were demonstrated to be higher than those of unilaterally ablated shrimps.
  • 5.5. The eyestalk-ablated shrimps possess higher total ATPase and Na+,K+-ATPase activities in the gill than those of unablated shrimps.
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20.
  • 1.1. Milk samples of 4 ml or more were obtained from guinea pigs (Cavia porcellus), dairy cattle (Bos taurus), horses (Equus caballus) and humans (Homo sapiens). The milks were analysed for minerals including calcium (Ca), phosphorus (P), magnesium (Mg), potassium (K) and sodium (Na) by Inductively Coupled Plasma-Optical Emission Spectroscopy (ICP-OES).
  • 2.2. Calcium was approximately twice as concentrated in guinea pig milk as in cows' milk, which was twice as much as the level in mares' milk, and this, in turn, was twice as concentrated as human milk.
  • 3.3. The ratio of Ca to P in guinea pig milk was 1.66:1, while it was 1.24:1 in cows' milk, 1.56:1 in mares' milk and 2.07:1 in human milk.
  • 4.4. Potassium was the most abundant mineral in the milks of cows, mares and humans, but not in guinea pig milk, and was much higher in cows' milk than in others.
  • 5.5. Sodium was highest in guinea pig milk with cows' milk being a close second.
  • 6.6. Magnesium was one-tenth as concentrated as Ca.
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